Acuhealth (USA) Pty., Ltd.
Country not established
- Devices
- 1
What Acuhealth (USA) Pty., Ltd. makes
Acuhealth (USA) Pty., Ltd. manufactures the TENS PRO 900, a transcutaneous electrical nerve stimulation (TENS) device designed for pain management through low-voltage electrical pulses.
The TENS PRO 900 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Tens Pro 900 Ref K915663
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acuhealth (Usa) Pty., Ltd. have in the registry?
The registry currently lists 1 device for Acuhealth (Usa) Pty., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acuhealth (Usa) Pty., Ltd.'s devices?
Among its 1 most recently registered device, Acuhealth (Usa) Pty., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Acuhealth (Usa) Pty., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Acuhealth (Usa) Pty., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acuhealth (Usa) Pty., Ltd. in the registry?
The most recently registered devices listed for Acuhealth (Usa) Pty., Ltd. include TENS PRO 900.